Bart Dermaut
- Full Professor
- Head of the Neurogenetics lab
Contact
Campus UZ, C. Heymanslaan 10, MRB2 (entrance 38), 9000 Ghent
E-mail I UGent Research Explorer | ORCID
Personalia
Biography
- 2018 - present: Full Professor - Ghent University
- 2018 - present: Clinical Geneticist - Ghent University Hospital
- 2011 - 2017: Associate Professor - Institut Pasteur de Lille (France)
- 2012 - 2018: Guest Professor - Ghent University
- 2007 - 2010: Postdoc - VIB-KU Leuven
- 2005 - 2007: Internship Neurology - Ghent University Hospital
- 2004 - 2005: Postdoc - VIB-Antwerp University
- 2002 - 2004: Postdoc - Baylor College of Medicine Houston (Texas)
- 2002: PhD - VIB-Antwerp University
- 1997: MD - Ghent University
Member of
- Center for Medical Genetics Ghent
- Solve-RD
- PrOZA - Ghent University Hospital
Promotor of
Research tracks
Expertise
- Clinical genetics and functional multi-omics of rare adult-onset neurodegenerative and neurological disorders.
Publications
Key publications
- Loss of phospholipase PLAAT3 causes a mixed lipodystrophic and neurological syndrome due to impaired PPARγ signaling. (2023) Nature Genetics.
- SRSF1 haploinsufficiency is responsible for a syndromic developmental disorder associated with intellectual disability. (2023) American Journal of Human Genetics.
- C-terminal frameshift variant of TDP-43 with pronounced aggregation-propensity causes rimmed vacuole myopathy but not ALS/FTD. (2023) Acta Neuropathologica.
- Tau promotes oxidative stress-associated cycling neurons in S phase as a pro-survival mechanism : possible implication for Alzheimer's disease. (2023) Progress in Neurobiology.
- Moyamoya disease emerging as an immune-related angiopathy. (2022) Trends in Molecular Medicine.